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纤维素底物的有效纤维素酶结合能力。

The productive cellulase binding capacity of cellulosic substrates.

作者信息

Karuna Nardrapee, Jeoh Tina

机构信息

Department of Biological and Agricultural Engineering, University of California, One Shields Ave., Davis 95616, California.

出版信息

Biotechnol Bioeng. 2017 Mar;114(3):533-542. doi: 10.1002/bit.26193. Epub 2016 Oct 13.

Abstract

Cellulosic biomass is the most promising feedstock for renewable biofuel production; however, the mechanisms of the heterogeneous cellulose saccharification reaction are still unsolved. As cellulases need to bind isolated molecules of cellulose at the surface of insoluble cellulose fibrils or larger aggregated cellulose structures in order to hydrolyze glycosidic bonds, the "accessibility of cellulose to cellulases" is considered to be a reaction limiting property of cellulose. We have defined the accessibility of cellulose to cellulases as the productive binding capacity of cellulose, that is, the concentration of productive binding sites on cellulose that are accessible for binding and hydrolysis by cellulases. Productive cellulase binding to cellulose results in hydrolysis and can be quantified by measuring hydrolysis rates. In this study, we measured the productive Trichoderma reesei Cel7A (TrCel7A) binding capacity of five cellulosic substrates from different sources and processing histories. Swollen filter paper and bacterial cellulose had higher productive binding capacities of ∼6 µmol/g while filter paper, microcrystalline cellulose, and algal cellulose had lower productive binding capacities of ∼3 µmol/g. Swelling and regenerating filter paper using phosphoric acid increased the initial accessibility of the reducing ends to TrCel7A from 4 to 6 µmol/g. Moreover, this increase in initial productive binding capacity accounted in large part for the difference in the overall digestibility between filter paper and swollen filter paper. We further demonstrated that an understanding of how the productive binding capacity declines over the course of the hydrolysis reaction has the potential to predict overall saccharification time courses. Biotechnol. Bioeng. 2017;114: 533-542. © 2016 Wiley Periodicals, Inc.

摘要

纤维素生物质是可再生生物燃料生产中最具前景的原料;然而,多相纤维素糖化反应的机制仍未解决。由于纤维素酶需要在不溶性纤维素原纤维或更大的聚集纤维素结构表面结合分离的纤维素分子,以便水解糖苷键,因此“纤维素对纤维素酶的可及性”被认为是纤维素的一种反应限制特性。我们将纤维素对纤维素酶的可及性定义为纤维素的有效结合能力,即纤维素上可被纤维素酶结合并水解的有效结合位点的浓度。纤维素酶与纤维素的有效结合会导致水解,并且可以通过测量水解速率来定量。在本研究中,我们测量了来自不同来源和加工历史的五种纤维素底物的里氏木霉Cel7A(TrCel7A)有效结合能力。膨胀滤纸和细菌纤维素具有较高的有效结合能力,约为6 μmol/g,而滤纸、微晶纤维素和藻类纤维素的有效结合能力较低,约为3 μmol/g。用磷酸对滤纸进行膨胀和再生,可使还原端对TrCel7A的初始可及性从4 μmol/g提高到6 μmol/g。此外,初始有效结合能力的这种提高在很大程度上解释了滤纸和膨胀滤纸之间总体消化率的差异。我们进一步证明,了解有效结合能力在水解反应过程中如何下降,有可能预测总体糖化时间进程。《生物技术与生物工程》2017年;114: 533 - 542。© 2016威利期刊公司

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